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rs876661208

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCTGGAGGTGCAG;GCTGGAGGTGCAG) 0 common in clinvar
Make rs876661208(-;-)
Make rs876661208(-;TGGAGGTGCAGGC)
Make rs876661208(TGGAGGTGCAGGC;TGGAGGTGCAGGC)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position127501100
GeneLRSAM1
is asnp
is mentioned by
dbSNPrs876661208
dbSNP (old)rs876661208
ClinGenrs876661208
ebirs876661208
HLIrs876661208
Exacrs876661208
Gnomadrs876661208
Varsomers876661208
Maprs876661208
PheGenIrs876661208
Biobankrs876661208
1000 genomesrs876661208
hgdprs876661208
ensemblrs876661208
gopubmedrs876661208
geneviewrs876661208
scholarrs876661208
googlers876661208
pharmgkbrs876661208
gwascentralrs876661208
openSNPrs876661208
23andMers876661208
23andMe allrs876661208
SNP Nexus

SNPshotrs876661208
SNPdbers876661208
MSV3drs876661208
GWAS Ctlgrs876661208
Max Magnitude0
ClinVar
Risk rs876661208(-;-)
Alt rs876661208(-;-)
Reference Rs876661208(GCTGGAGGTGCAG;GCTGGAGGTGCAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LRSAM1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.130263379_130263391delTGGAGGTGCAGGC
CLNSRC
CLNACC RCV000214054.1,